Canonical Allele Identifier: CA2474156941
Gene: NSUN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46368595C= , CM000663.2:g.46368595C= GRCh38
NC_000001.10:g.46834267C= , CM000663.1:g.46834267C= GRCh37
NC_000001.9:g.46606854C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001387266.1:c.*726C= NP_001374195.1:n.*726C=
NM_001387268.1:c.1006-177C= NP_001374197.1:n.1006-177C=
NM_001387269.1:c.*207C= NP_001374198.1:n.*207C=
NM_001387270.1:c.878+7767C= NP_001374199.1:n.878+7767C=